Synthesis of propargylamine mycophenolate analogues and their selective cytotoxic activity towards neuroblastoma SH-SY5Y cell line-Reference-Cited by-同舟云学术

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Synthesis of propargylamine mycophenolate analogues and their selective cytotoxic activity towards neuroblastoma SH-SY5Y cell line

Published:2021-08 Issue: Volume:45 Page:128135
ISSN:0960-894X
Container-title:Bioorganic & Medicinal Chemistry Letters
language:en
Short-container-title:Bioorganic & Medicinal Chemistry Letters

Author:

Silalai Patamawadee,Pruksakorn Dumnoensun,Chairoungdua Arthit,Suksen Kanoknetr,Saeeng Rungnapha

Funder

Burapha University

Center of Excellence for Innovation in Chemistry

National Research Council of Thailand

Publisher

Elsevier BV

Reference46 articles.

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2. Design, synthesis, and biological evaluation of NAD(P)H: Quinone oxidoreductase (NQO1)-targeted oridonin prodrugs possessing indolequinone moiety for hypoxia-selective activation;Xu;Eur J Med Chem.,2017

3. Epigallocatechin gallate-zinc oxide co-crystalline nanoparticles as an anticancer drug that is non-toxic to normal cells;Samutprasert;RSC Adv,2018

4. Neuroblastoma;Ishola;Surg Oncol,2007

5. Comparison of conventional to intensity modulated radiation therapy for abdominal neuroblastoma;Paulino;Pediatr Blood Cancer,2006

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4. Cu‐Catalyzed Cross‐Coupling Reactions of Enamines and Terminal Alkynes: Access of Propargylamines as Neurodegenerative Disorder Agents;Asian Journal of Organic Chemistry;2023-09-12

5. 2-{[4-(4-Bromophenyl)piperazin-1-yl)]methyl}-4-(3-chlorophenyl)-5-(4-methoxyphenyl)-2,4-dihydro-3H-1,2,4-triazole-3-thione;Molbank;2023-01-12

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